Temporal dynamics of triphasic waves and generalized periodic discharges
George Plummer1, Ryan Raut1, Bingni Brunton1, Shahin Hakimian2
1University of Washington, 2UW Regional Epilepsy Center At Harborview
Objective:

To quantitatively compare triphasic waves and generalized periodic discharges on scalp EEG.

Background:

Distinguishing epileptiform generalized periodic discharges (GPDs) and triphasic waves (TWs) can be challenging (Foreman et al., 2016), and consequential since groups may benefit from anti-seizure medications differently. Discharge regularity is an important feature recapitulated in computational models of TWs (Song et al., 2019) and GPDs (Ruijter et al., 2017). Recent analysis of GPDs in patients after cardiac arrest have shown that regularity of GPD duration, morphology, and amplitude, based on visual scoring, portend worse prognoses (Nadjar et al., 2022). This suggests that variability of discharges could be a quantifiable tool in distinguishing GPDs from TWs.

Design/Methods:

We retrospectively collected inpatient EEG recordings marked to show GPDs and TWs from Harborview Medical Center between 11/2020 and 5/2021. The best derivation of a 30 second artifact free period on average reference montage was low pass filtered (0-15hz) for analysis. After visually identifying discharges, interdischarge intervals (IDIs) were calculated based on maximal deflection of each discharge. For each EEG, variance of IDIs was normalized by median IDI, to calculate a regularity index (RI). RI of GPDs and TWs were compared with a one-tailed Wilcoxon rank sum test.

Results:

24 EEGs with TWs and 33 EEGs with GPDs were studied. Median RI for TWs was 0.438 with a variance of 3.08. Median RI for GPDs was 0.368 with a variance of 4.31. Groups were not statistically different (p=0.08). Excluding EEGs of following cardiac arrest, 23 EEGs with TWs and 10 EEGs with GPDs were studied. Median RI of TWs was 0.430 with variance of 3.14. Median RI of GPDs was 3.14 with variance of 13.7. Groups were not statistically different (p=0.27).

Conclusions:

Comparison of normalized variability in IDI does not distinguish TWs from GPDs but may have utility in the context of other clinical data.

10.1212/WNL.0000000000201863